Re: (unknown)

[Guest guest]

I do remember you. I am also very upset with your situation. I don't believe that there should be a time limit on suing these bastards. Not ONE lawyer would take my case. I must have spoke to 20 or 30 of them. That is the great thing about living in the us. The working class gets raped by the government while the government subsidizes big pharma, big banks, big autos, with working class tax money. They care not about individual unless they are worth millions. My thoughts and prayers are with you.Warmest Regards,TonySent from my iPadOn Mar 28, 2011, at 10:36 PM, Whoami Dontknow <deana729@...> wrote:

Hello all,

If anyone remembers me, I lost my dad to what we feel was a effexor induced suicide. We tried to get a lawsuit together and after two lawyers led us to believe they would take our case they both ended up dropping them last minute before our filing period was up. One due to pre-emption and one decided to take only take cases of children.

So, here we are after the time allowed to file and are trying to pick up the pieces and find anyway to get justice for my dad since we can not get the drug companies to acknowledge that these medicines work against some people. It deeply hurts to know this and that others will possibly get the same results as my dad. Does anyone have any suggestions to help spread the word or any way to help? Anything. These drugs are so dangerous.

[Guest guest]

I do remember you. I am also very upset with your situation. I don't believe that there should be a time limit on suing these bastards. Not ONE lawyer would take my case. I must have spoke to 20 or 30 of them. That is the great thing about living in the us. The working class gets raped by the government while the government subsidizes big pharma, big banks, big autos, with working class tax money. They care not about individual unless they are worth millions. My thoughts and prayers are with you.Warmest Regards,TonySent from my iPadOn Mar 28, 2011, at 10:36 PM, Whoami Dontknow <deana729@...> wrote:

Hello all,

If anyone remembers me, I lost my dad to what we feel was a effexor induced suicide. We tried to get a lawsuit together and after two lawyers led us to believe they would take our case they both ended up dropping them last minute before our filing period was up. One due to pre-emption and one decided to take only take cases of children.

So, here we are after the time allowed to file and are trying to pick up the pieces and find anyway to get justice for my dad since we can not get the drug companies to acknowledge that these medicines work against some people. It deeply hurts to know this and that others will possibly get the same results as my dad. Does anyone have any suggestions to help spread the word or any way to help? Anything. These drugs are so dangerous.

[Guest guest]

I do remember you. I am also very upset with your situation. I don't believe that there should be a time limit on suing these bastards. Not ONE lawyer would take my case. I must have spoke to 20 or 30 of them. That is the great thing about living in the us. The working class gets raped by the government while the government subsidizes big pharma, big banks, big autos, with working class tax money. They care not about individual unless they are worth millions. My thoughts and prayers are with you.Warmest Regards,TonySent from my iPadOn Mar 28, 2011, at 10:36 PM, Whoami Dontknow <deana729@...> wrote:

Hello all,

If anyone remembers me, I lost my dad to what we feel was a effexor induced suicide. We tried to get a lawsuit together and after two lawyers led us to believe they would take our case they both ended up dropping them last minute before our filing period was up. One due to pre-emption and one decided to take only take cases of children.

So, here we are after the time allowed to file and are trying to pick up the pieces and find anyway to get justice for my dad since we can not get the drug companies to acknowledge that these medicines work against some people. It deeply hurts to know this and that others will possibly get the same results as my dad. Does anyone have any suggestions to help spread the word or any way to help? Anything. These drugs are so dangerous.

[Guest guest]

Hi AdelaI just spoke to Sophie. She said please call her on Wednesday, between 10pm and 4pm UK time. She suggested that you also send a photo and email, so she can forward it to Mr Collin.Please tell me if you need further help from me. Take care, Shireen From: blepharophimosis [mailto:blepharophimosis ] On Behalf Of Shireen MohandesSent: 26 March 2011 14:24blepharophimosis Subject: RE: blepharophimosis (unknown) Dear AdelaI will try to phone her again on Monday, I tried on Friday but did not get through to her.I am sure that I can help you be in touch with each other.Take careShireen From: blepharophimosis [mailto:blepharophimosis ] On Behalf Of adela todericiSent: 26 March 2011 13:58blepharophimosis Subject: RE: blepharophimosis (unknown) Sorry! I realized that I was not presented.My name is Adela Constantinescu and I'm from Romania I tried to talk to Mr Collin secretary, but I could not, I'll try again.Thank you very much!From: Shireen Mohandes <shireen@...>Subject: RE: blepharophimosis (unknown)blepharophimosis Date: Thursday, March 24, 2011, 10:00 AM I just realised, the 23rd March was yesterday. Perhaps they will be there tomorrow morning. I will try again. From: blepharophimosis [mailto:blepharophimosis ] On Behalf Of Shireen MohandesSent: 24 March 2011 16:45blepharophimosis Subject: RE: blepharophimosis (unknown) Dear Todericiadele (I am sorry I don’t know your name)One of the best specialists in opthalmoplastic surgery is a surgeon called Mr Collin.Here is a link.I tried to call his secretary but the office is closed until 23rd March.I am sure that if you contact him, via his secretary, I think her name is Sophie Tay 020 7486 2699, then you can get some more information. Mr Colin may be able to suggest a specialist who is geographically closer to your home. The email is: info@... In the email subject put “FAO Mr Collin†Let us know how you get on and if you need more help. Mr Collin is very friendly, and one of the top 5 experts in the world for this type of surgery. Regards, Shireen London, England From: blepharophimosis [mailto:blepharophimosis ] On Behalf Of todericiadelaSent: 24 March 2011 15:10blepharophimosis Subject: blepharophimosis (unknown) Hello!I'm from Romania and a girl of only 10 months, eye problems (BPES). I am very worried for her, I want the best for her, so I have a REQUEST from you if you let me suggest a clinic, the good doctor (preferably in Europe) and how such operations cost.Thanks very much!

[Guest guest]

Oh my gosh, you couldn't have said anything more that would scare the begeebers

out of me! My son has seizures and I am hoping they will get better with Dr G's

protocol. So, listmates, PLEASE weigh in on this.

Thanks,

Sheryl

Sent from my iPh

On Mar 29, 2011, at 7:56 PM, " chrissie.donlin " <chrissie.donlin@...>

wrote:

> my son is a patient of Dr.G's and we have had a horrible time starting the

SSRI's. Both times we have ended up in the hospital because the seizures start

and don't stop. Has this happened to anyone else?

>

>

[Guest guest]

We had some grand mal seizures prior to the protocol and none after a few

months in. Many many parents over the years have reported all seizure activity

stopped shortly after starting the protocol. I have never ever heard a parent

report any kind of increase of seizure activity on (it is possible they did

not post about it if they did), is it possible the SSRI is reacting badly and

possibly trying another would be best.

________________________________

From: Sheryl <ssaturnino@...>

" " < >

Cc: " " < >

Sent: Wed, March 30, 2011 12:31:39 AM

Subject: Re: (unknown)

Oh my gosh, you couldn't have said anything more that would scare the begeebers

out of me! My son has seizures and I am hoping they will get better with Dr G's

protocol. So, listmates, PLEASE weigh in on this.

Thanks,

Sheryl

Sent from my iPh

On Mar 29, 2011, at 7:56 PM, " chrissie.donlin " <chrissie.donlin@...>

wrote:

> my son is a patient of Dr.G's and we have had a horrible time starting the

>SSRI's. Both times we have ended up in the hospital because the seizures start

>and don't stop. Has this happened to anyone else?

>

>

[Guest guest]

Thank you, Bill.

Sent from my iPhone

On Mar 30, 2011, at 3:04 AM, Bill klimas <klimas_bill@...> wrote:

> We had some grand mal seizures prior to the protocol and none after a few

> months in. Many many parents over the years have reported all seizure activity

> stopped shortly after starting the protocol. I have never ever heard a parent

> report any kind of increase of seizure activity on (it is possible they

did

> not post about it if they did), is it possible the SSRI is reacting badly and

> possibly trying another would be best.

>

> ________________________________

> From: Sheryl <ssaturnino@...>

> " " < >

> Cc: " " < >

> Sent: Wed, March 30, 2011 12:31:39 AM

> Subject: Re: (unknown)

>

> Oh my gosh, you couldn't have said anything more that would scare the

begeebers

> out of me! My son has seizures and I am hoping they will get better with Dr

G's

> protocol. So, listmates, PLEASE weigh in on this.

>

> Thanks,

> Sheryl

>

> Sent from my iPh

>

> On Mar 29, 2011, at 7:56 PM, " chrissie.donlin " <chrissie.donlin@...>

> wrote:

>

> > my son is a patient of Dr.G's and we have had a horrible time starting the

> >SSRI's. Both times we have ended up in the hospital because the seizures

start

> >and don't stop. Has this happened to anyone else?

> >

> >

>

>

[Guest guest]

My son, too, had seizures prior to starting the protocol (he started when

he was 3.5) but they all stopped within a couple of weeks on the protocol.

Kristy Nardini

Tazzini Stainless Steel Bottles

www.tazzini.com

kristy@...

858.243.1929

<http://www.facebook.com/tazzinicompany> Find us on Facebook!

<http://www.twitter.com/tazzini> Follow us on Twitter!

From: [mailto: ] On Behalf Of Sheryl

Sent: Wednesday, March 30, 2011 7:25 AM

Subject: Re: (unknown)

Thank you, Bill.

Sent from my iPhone

On Mar 30, 2011, at 3:04 AM, Bill klimas <klimas_bill@...

<mailto:klimas_bill%40> > wrote:

> We had some grand mal seizures prior to the protocol and none after a few

> months in. Many many parents over the years have reported all seizure activity

> stopped shortly after starting the protocol. I have never ever heard a parent

> report any kind of increase of seizure activity on (it is possible they

did

> not post about it if they did), is it possible the SSRI is reacting badly and

> possibly trying another would be best.

>

> ________________________________

> From: Sheryl <ssaturnino@... <mailto:ssaturnino%40> >

> " <mailto:%40> "

< <mailto:%40> >

> Cc: " <mailto:%40> "

< <mailto:%40> >

> Sent: Wed, March 30, 2011 12:31:39 AM

> Subject: Re: (unknown)

>

> Oh my gosh, you couldn't have said anything more that would scare the

begeebers

> out of me! My son has seizures and I am hoping they will get better with Dr

G's

> protocol. So, listmates, PLEASE weigh in on this.

>

> Thanks,

> Sheryl

>

> Sent from my iPh

>

> On Mar 29, 2011, at 7:56 PM, " chrissie.donlin " <chrissie.donlin@...

<mailto:chrissie.donlin%40> >

> wrote:

>

> > my son is a patient of Dr.G's and we have had a horrible time starting the

> >SSRI's. Both times we have ended up in the hospital because the seizures

start

> >and don't stop. Has this happened to anyone else?

> >

> >

>

>

[Guest guest]

My son had a horrific seizure episode about 2 weeks before our first visit

to Dr. G. He has been on seizure meds since then ­ we had one breakthrough

seizure 2 months into the protocol and none since. We did not have any

issues starting an SSRI. Dr. G did want to try Wellbutrin, but I read that

one of the side effects (first one listed) was possible seizures and we both

thought it was not worth it to try as we are going to wean off of seizure

meds this November. I didn¹t want to have to wait another 2 years to get

off the seizure meds so he opted for something else.

I would send an email to the office or call the office and get an opinion on

that and/or read the package insert of the SSRI that has caused this and see

if it¹s a known side effect of that particular SSRI. Perhaps it¹s not an

appropriate one for your child or you might have to wait a little longer for

some healing before trying a SSRI again. I would get his opinion on what

the issue might be.

Laureen

On 3/30/11 6:54 AM, " Kristy Nardini " <knardini@...> wrote:

>

>

>

>

>

> My son, too, had seizures prior to starting the protocol (he started when

> he was 3.5) but they all stopped within a couple of weeks on the protocol.

>

> Kristy Nardini

>

> Tazzini Stainless Steel Bottles

>

> www.tazzini.com

>

> kristy@... <mailto:kristy%40tazzini.com>

>

> 858.243.1929

>

> <http://www.facebook.com/tazzinicompany> Find us on Facebook!

>

> <http://www.twitter.com/tazzini> Follow us on Twitter!

>

> From: <mailto:%40>

> [mailto: <mailto:%40> ] On Behalf Of

> Sheryl

> Sent: Wednesday, March 30, 2011 7:25 AM

> <mailto:%40>

> Subject: Re: (unknown)

>

> Thank you, Bill.

>

> Sent from my iPhone

>

> On Mar 30, 2011, at 3:04 AM, Bill klimas <klimas_bill@...

> <mailto:klimas_bill%40> <mailto:klimas_bill%40> > wrote:

>

>> > We had some grand mal seizures prior to the protocol and none after a

>> few

>> > months in. Many many parents over the years have reported all seizure

>> activity

>> > stopped shortly after starting the protocol. I have never ever heard a

>> parent

>> > report any kind of increase of seizure activity on (it is possible

>> they did

>> > not post about it if they did), is it possible the SSRI is reacting badly

>> and

>> > possibly trying another would be best.

>> >

>> > ________________________________

>> > From: Sheryl <ssaturnino@... <mailto:ssaturnino%40>

>> <mailto:ssaturnino%40> >

>> > " <mailto:%40>

>> <mailto:%40> " <

>> <mailto:%40> <mailto:%40> >

>> > Cc: " <mailto:%40>

>> <mailto:%40> " <

>> <mailto:%40> <mailto:%40> >

>> > Sent: Wed, March 30, 2011 12:31:39 AM

>> > Subject: Re: (unknown)

>> >

>> > Oh my gosh, you couldn't have said anything more that would scare the

>> begeebers

>> > out of me! My son has seizures and I am hoping they will get better with Dr

>> G's

>> > protocol. So, listmates, PLEASE weigh in on this.

>> >

>> > Thanks,

>> > Sheryl

>> >

>> > Sent from my iPh

>> >

>> > On Mar 29, 2011, at 7:56 PM, " chrissie.donlin " <chrissie.donlin@...

>> <mailto:chrissie.donlin%40> <mailto:chrissie.donlin%40> >

>> > wrote:

>> >

>>> > > my son is a patient of Dr.G's and we have had a horrible time starting

>>> the

>>> > >SSRI's. Both times we have ended up in the hospital because the seizures

>>> start

>>> > >and don't stop. Has this happened to anyone else?

>>> > >

>>> > >

>> >

>> >

[Guest guest]

We had the same issue, but it went away after a few weeks. Every time we change

meds the same thing happens. I put a towel down as a precaution.

Sent from my iPhone

On Mar 30, 2011, at 1:23 AM, YADI AGUIN <yadi1007@...> wrote:

> hi, my son has been on the protocol for 18 months and since we started

the ssri's he's had night wetting almost every single night. it's very

frustrating since he was fully trained before. I had to get him back on pull ups

since it just got very overwhelming getting him up every night and still he

would get back to bed and pee on his bed again.

>

>

[Guest guest]

jim it said that this was an affect file

________________________________

From: Garrison <jwg4659@...>

csavage@...; Joint Replacement ; jwg4659@...;

bruckesan@...; FreecycleLickingCountyOhio-owner ;

shawdawn78@...; security@...; annaberry21@...;

Kgarrison5@...

Sent: Wed, March 30, 2011 11:40:14 PM

Subject: (unknown)

http://www.sfcusainc.com/images/acc.php

[Guest guest]

Anytime you see an email that has no subject line and then has a link to

a website within it, BE CAREFUL. It is usually a virus.

Eileen Ann Edelblute

Clinton, MD

My Journey to pain free knees

http://mysite.verizon.net/vze88xkr/id30.html

Re: (unknown)

jim it said that this was an affect file

[Guest guest]

I have really been loving making almond milk! I especially LOVE it in my oatmeal! FrannyOn Mar 7, 2011, at 4:00 AM, le Meyer wrote:

I can't wait to try almond milk in my VM.

[Guest guest]

Have any of you heard about this new drug that is suppose to have 70% cure

rate for Hep C? My dad was hearing something about it on the news. Heck I

am so busy with work and kids I never have time to do research anymore lol.

Just wondering ?

From: Hepatitis C

[mailto:Hepatitis C ] On Behalf Of deborah brown

Sent: Wednesday, March 30, 2011 10:31 AM

Hepatitis C

Cc: deborah kay mand

Subject: (unknown)

http://www.teatronaturale.com/article/2390.html <Liquorice bennifits!

[Guest guest]

Thanks to the replies I received. If anyone wants to send me a private email please feel free to do so also with any information or ideas. I will continue to try to find ways to warn others on what happened to my dad. I just feel for those that are going thru what we already have since the drug companies dont seem to care about the people that get these "bad side effects" as they call them. Also the doctors that hand them out like candy.

From: Whoami Dontknow <deana729@...>SSRI medications ; SSRI medications Sent: Mon, March 28, 2011 7:36:22 PMSubject: (unknown)

Hello all,

If anyone remembers me, I lost my dad to what we feel was a effexor induced suicide. We tried to get a lawsuit together and after two lawyers led us to believe they would take our case they both ended up dropping them last minute before our filing period was up. One due to pre-emption and one decided to take only take cases of children.

So, here we are after the time allowed to file and are trying to pick up the pieces and find anyway to get justice for my dad since we can not get the drug companies to acknowledge that these medicines work against some people. It deeply hurts to know this and that others will possibly get the same results as my dad. Does anyone have any suggestions to help spread the word or any way to help? Anything. These drugs are so dangerous.

[Guest guest]

Thanks to the replies I received. If anyone wants to send me a private email please feel free to do so also with any information or ideas. I will continue to try to find ways to warn others on what happened to my dad. I just feel for those that are going thru what we already have since the drug companies dont seem to care about the people that get these "bad side effects" as they call them. Also the doctors that hand them out like candy.

From: Whoami Dontknow <deana729@...>SSRI medications ; SSRI medications Sent: Mon, March 28, 2011 7:36:22 PMSubject: (unknown)

Hello all,

If anyone remembers me, I lost my dad to what we feel was a effexor induced suicide. We tried to get a lawsuit together and after two lawyers led us to believe they would take our case they both ended up dropping them last minute before our filing period was up. One due to pre-emption and one decided to take only take cases of children.

So, here we are after the time allowed to file and are trying to pick up the pieces and find anyway to get justice for my dad since we can not get the drug companies to acknowledge that these medicines work against some people. It deeply hurts to know this and that others will possibly get the same results as my dad. Does anyone have any suggestions to help spread the word or any way to help? Anything. These drugs are so dangerous.

[Guest guest]

Thanks to the replies I received. If anyone wants to send me a private email please feel free to do so also with any information or ideas. I will continue to try to find ways to warn others on what happened to my dad. I just feel for those that are going thru what we already have since the drug companies dont seem to care about the people that get these "bad side effects" as they call them. Also the doctors that hand them out like candy.

From: Whoami Dontknow <deana729@...>SSRI medications ; SSRI medications Sent: Mon, March 28, 2011 7:36:22 PMSubject: (unknown)

Hello all,

If anyone remembers me, I lost my dad to what we feel was a effexor induced suicide. We tried to get a lawsuit together and after two lawyers led us to believe they would take our case they both ended up dropping them last minute before our filing period was up. One due to pre-emption and one decided to take only take cases of children.

So, here we are after the time allowed to file and are trying to pick up the pieces and find anyway to get justice for my dad since we can not get the drug companies to acknowledge that these medicines work against some people. It deeply hurts to know this and that others will possibly get the same results as my dad. Does anyone have any suggestions to help spread the word or any way to help? Anything. These drugs are so dangerous.

[Guest guest]

Thanks to the replies I received. If anyone wants to send me a private email please feel free to do so also with any information or ideas. I will continue to try to find ways to warn others on what happened to my dad. I just feel for those that are going thru what we already have since the drug companies dont seem to care about the people that get these "bad side effects" as they call them. Also the doctors that hand them out like candy.

From: Whoami Dontknow <deana729@...>SSRI medications ; SSRI medications Sent: Mon, March 28, 2011 7:36:22 PMSubject: (unknown)

Hello all,

If anyone remembers me, I lost my dad to what we feel was a effexor induced suicide. We tried to get a lawsuit together and after two lawyers led us to believe they would take our case they both ended up dropping them last minute before our filing period was up. One due to pre-emption and one decided to take only take cases of children.

So, here we are after the time allowed to file and are trying to pick up the pieces and find anyway to get justice for my dad since we can not get the drug companies to acknowledge that these medicines work against some people. It deeply hurts to know this and that others will possibly get the same results as my dad. Does anyone have any suggestions to help spread the word or any way to help? Anything. These drugs are so dangerous.

[Guest guest]

AcylicFrom: Aqsa Fatima Burki <aqsaburki@...>Subject: (unknown) Date: Saturday, 2 April, 2011, 8:35 PM

What are the artificial teeth in removable dentures made of?A.PorcelainB.Cross-linked methyl-methacrylateC.Ethyl-methacrylateD.Acrylic

[Guest guest]

hi em, i did here something awhile ago about a drug they were testing that had

nothing to do with the treatments they use now and that theres very few side

effects,but never really checked into it. Summers coming... Horraaaaay

From: Haj <emily_sweethang@...>

Subject: RE: (unknown)

Hepatitis C

Date: Friday, April 1, 2011, 7:33 AM

 

Have any of you heard about this new drug that is suppose to have 70% cure

rate for Hep C? My dad was hearing something about it on the news. Heck I

am so busy with work and kids I never have time to do research anymore lol.

Just wondering ?

From: Hepatitis C

[mailto:Hepatitis C ] On Behalf Of deborah brown

Sent: Wednesday, March 30, 2011 10:31 AM

Hepatitis C

Cc: deborah kay mand

Subject: (unknown)

http://www.teatronaturale.com/article/2390.html <Liquorice bennifits!

[Guest guest]

I have to agree, if can all come together from the standpoint that our

children are medically ill, there are things that are out there to help now,

it would be better received than placing blame. Then, once the medical

establishments sees the real change in our kids, they will be more likely to

want to research further to find agents to help.

I¹ve often found that in the ³A² community such differences in beliefs of

the causative factor has polarized this population and has not helped to

advance real change. I can¹t worry right now about what the cause

is/was/may be, I want help now to treat my sons medical illness for him to

get better to lead a productive life. I also really believe in this current

economy that if we can show that these kids eventually stop needing

services, can go to school and get jobs and become contributing members of

society, that would resonate with the legislators in this country as well.

We all know that they are looking to slash services for our kids due to

budgets ­ what if, these kids start getting better and don¹t need

entitlement programs anymore?

I, for one, really believe that if we can get the ³A² word kids out of the

DSMIV and into the medical illness category, there is real possibility for

help and better lives for these kids and/or adults.

Laureen

On 4/2/11 6:56 PM, " Lynn Capone " <ecapne@...> wrote:

>

>

>

>

>

> Hi everyone.

>  

> I know that as a group, we all do not agree on what causes autism but can

> probably attest

> that our kids need help and need the medical community to really focus on

> treatments for

> what the group has evidence is an immune related disorder.  For Autism

> Awareness, we are urging that people contact the American Academy of

> Pediatrics to start a campaign to demand treatment.  I know that there have

> been many studies regarding the role of vaccines but as a group, we believe

> that although a safe and/or delayed vaccine schedule is important but

> continuing to study this role will not help us produce treatments to help our

> children now as they are for what I think a lot of us could describe as a

> disease due to physical symptoms, typical development and then regression,

> etc,  that were are not present in cases of Kanner autism.  Also, the numbers

> of diagnosed cases is increasing expotentially and this cannot be explained by

> a developmental disorder otherwise other developmental disabilities would be

> seeing the same increases.

>  

> So with an open mind, I urge you to visit the site and if you disagree,

> perhaps we can agree that as parents we need to take action and advocate for

> our children because we would not be part of this group unless what we share

> is that we are devoted.

>  

> Here is the website:  http://www.nids.net

>  

> I would urge you to take some time to read through the site and help us

> advocate for our children by writing to the Academy of Pediatrics (as listed

> at the bottom of the website), your pediatricians, visiting us on Facebook

> under , etc. It is understandable that we are all busy and stressed out

> with our daily lives, but I urge all of you as parents to take the time to

> join us so that we could positively affect our children's future.  It is worth

> a shot but I would mention that if we speak about vaccines, we will continue

> to be ignored.  Again, I am not saying that this is not a trigger, but this

> issue has been so polarizing and basically written off by the Academy that I

> can guarantee you that if we approach it in this matter, nothing will be done

> for our children.    Let's focus on getting them better now   If the medical

> community can cure Polio, prolong the lives of people afflicted with AIDS, and

> almost wipe  out or manage other

> diseases, why can it not be autism?? If like me, you are worried about the

> future for your child or children, why not give it a try? 

>  

>  Dr. Goldberg has had many success cases and the specifics are outlined in his

> book The Myth of Autism.  Even with the success that he has had with many of

> his cases  and believe me, he and his wife are absolutely dedicated to this

> cause, he realizes that there is a large portion of the population that

> responds to his protocol, but needs better standard treatment in order to

> advance further.

>  

> Have a nice night.

>  

>  

> Lynn

>

>

[Guest guest]

I think your father's story is very important

because the psychiatrists and drug makers would have us all

believe there is no risk after 24 years old.

Was your father diagnosed with depression or some other "mental

illness"? Either way your story is important but the pharma guys

will blame the patient as usual. If your father was given the drug

for chest pain for example then you have the gold plated silver

magic bullet and it would be a crying shame not to warn people

with your fathers tragedy.

best,

Jim

On 4/1/2011 7:58 PM, Whoami Dontknow wrote:

Thanks to the replies I received. If anyone wants to send

me a private email please feel free to do so also with any

information or ideas. I will continue to try to find ways to

warn others on what happened to my dad. I just feel for those

that are going thru what we already have since the drug

companies dont seem to care about the people that get these

"bad side effects" as they call them. Also the doctors that

hand them out like candy.

From:

Whoami Dontknow <deana729@...>

To:

SSRI medications ;

SSRI medications

Sent: Mon,

March 28, 2011 7:36:22 PM

Subject:

(unknown)

 

Hello all,

 

If anyone remembers me, I lost my dad to what we

feel was a effexor induced suicide. We tried to get a

lawsuit together and after two lawyers led us to

believe they would take our case they both ended up

dropping them last minute before our filing period was

up. One due to pre-emption and one decided to take

only take cases of children.

So, here we are after the time allowed to file and

are trying to pick up the pieces and find anyway to

get justice for my dad since we can not get the drug

companies to acknowledge that these medicines work

against some people. It deeply hurts to know this and

that others will possibly get the same results as my

dad. Does anyone have any suggestions to help spread

the word or any way to help? Anything. These drugs are

so dangerous.

[Guest guest]

I think your father's story is very important

because the psychiatrists and drug makers would have us all

believe there is no risk after 24 years old.

Was your father diagnosed with depression or some other "mental

illness"? Either way your story is important but the pharma guys

will blame the patient as usual. If your father was given the drug

for chest pain for example then you have the gold plated silver

magic bullet and it would be a crying shame not to warn people

with your fathers tragedy.

best,

Jim

On 4/1/2011 7:58 PM, Whoami Dontknow wrote:

Thanks to the replies I received. If anyone wants to send

me a private email please feel free to do so also with any

information or ideas. I will continue to try to find ways to

warn others on what happened to my dad. I just feel for those

that are going thru what we already have since the drug

companies dont seem to care about the people that get these

"bad side effects" as they call them. Also the doctors that

hand them out like candy.

From:

Whoami Dontknow <deana729@...>

To:

SSRI medications ;

SSRI medications

Sent: Mon,

March 28, 2011 7:36:22 PM

Subject:

(unknown)

 

Hello all,

 

If anyone remembers me, I lost my dad to what we

feel was a effexor induced suicide. We tried to get a

lawsuit together and after two lawyers led us to

believe they would take our case they both ended up

dropping them last minute before our filing period was

up. One due to pre-emption and one decided to take

only take cases of children.

So, here we are after the time allowed to file and

are trying to pick up the pieces and find anyway to

get justice for my dad since we can not get the drug

companies to acknowledge that these medicines work

against some people. It deeply hurts to know this and

that others will possibly get the same results as my

dad. Does anyone have any suggestions to help spread

the word or any way to help? Anything. These drugs are

so dangerous.

[Guest guest]

I think your father's story is very important

because the psychiatrists and drug makers would have us all

believe there is no risk after 24 years old.

Was your father diagnosed with depression or some other "mental

illness"? Either way your story is important but the pharma guys

will blame the patient as usual. If your father was given the drug

for chest pain for example then you have the gold plated silver

magic bullet and it would be a crying shame not to warn people

with your fathers tragedy.

best,

Jim

On 4/1/2011 7:58 PM, Whoami Dontknow wrote:

Thanks to the replies I received. If anyone wants to send

me a private email please feel free to do so also with any

information or ideas. I will continue to try to find ways to

warn others on what happened to my dad. I just feel for those

that are going thru what we already have since the drug

companies dont seem to care about the people that get these

"bad side effects" as they call them. Also the doctors that

hand them out like candy.

From:

Whoami Dontknow <deana729@...>

To:

SSRI medications ;

SSRI medications

Sent: Mon,

March 28, 2011 7:36:22 PM

Subject:

(unknown)

 

Hello all,

 

If anyone remembers me, I lost my dad to what we

feel was a effexor induced suicide. We tried to get a

lawsuit together and after two lawyers led us to

believe they would take our case they both ended up

dropping them last minute before our filing period was

up. One due to pre-emption and one decided to take

only take cases of children.

So, here we are after the time allowed to file and

are trying to pick up the pieces and find anyway to

get justice for my dad since we can not get the drug

companies to acknowledge that these medicines work

against some people. It deeply hurts to know this and

that others will possibly get the same results as my

dad. Does anyone have any suggestions to help spread

the word or any way to help? Anything. These drugs are

so dangerous.

[Guest guest]

I think your father's story is very important

because the psychiatrists and drug makers would have us all

believe there is no risk after 24 years old.

Was your father diagnosed with depression or some other "mental

illness"? Either way your story is important but the pharma guys

will blame the patient as usual. If your father was given the drug

for chest pain for example then you have the gold plated silver

magic bullet and it would be a crying shame not to warn people

with your fathers tragedy.

best,

Jim

On 4/1/2011 7:58 PM, Whoami Dontknow wrote:

Thanks to the replies I received. If anyone wants to send

me a private email please feel free to do so also with any

information or ideas. I will continue to try to find ways to

warn others on what happened to my dad. I just feel for those

that are going thru what we already have since the drug

companies dont seem to care about the people that get these

"bad side effects" as they call them. Also the doctors that

hand them out like candy.

From:

Whoami Dontknow <deana729@...>

To:

SSRI medications ;

SSRI medications

Sent: Mon,

March 28, 2011 7:36:22 PM

Subject:

(unknown)

 

Hello all,

 

If anyone remembers me, I lost my dad to what we

feel was a effexor induced suicide. We tried to get a

lawsuit together and after two lawyers led us to

believe they would take our case they both ended up

dropping them last minute before our filing period was

up. One due to pre-emption and one decided to take

only take cases of children.

So, here we are after the time allowed to file and

are trying to pick up the pieces and find anyway to

get justice for my dad since we can not get the drug

companies to acknowledge that these medicines work

against some people. It deeply hurts to know this and

that others will possibly get the same results as my

dad. Does anyone have any suggestions to help spread

the word or any way to help? Anything. These drugs are

so dangerous.